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The Nuclear IκB Protein IκBNS Selectively Inhibits Lipopolysaccharide-Induced IL-6 Production in Macrophages of the Colonic Lamina Propria
Open accessAbstract
Macrophages play an important role in the pathogenesis of chronic colitis. However, it remains unknown how macrophages residing in the colonic lamina propria are regulated. We characterized colonic lamina proprial CD11b-positive cells (CLPMφ). CLPMφ of wild-type mice, but not IL-10-deficient mice, displayed hyporesponsiveness to TLR stimulation in terms of cytokine production and costimulatory molecule expression. We compared CLPMφ gene expression profiles of wild-type mice with IL-10-deficient mice, and identified genes that are selectively expressed in wild-type CLPMφ. These genes included nuclear IκB proteins such as Bcl-3 and IκBNS. Because Bcl-3 has been shown to specifically inhibit LPS-induced TNF-α production, we analyzed the role of IκBNS in macrophages. Lentiviral introduction of IκBNS resulted in impaired LPS-induced IL-6 production, but not TNF-α production in the murine macrophage cell line RAW264.7. IκBNS expression led to constitutive and intense DNA binding of NF-κB p50/p50 homodimers. IκBNS was recruited to the IL-6 promoter, but not to the TNF-α promoter, together with p50. Furthermore, small interference RNA-mediated reduction in IκBNS expression in RAW264.7 cells resulted in increased LPS-induced production of IL-6, but not TNF-α. Thus, IκBNS selectively suppresses LPS-induced IL-6 production in macrophages. This study established that nuclear IκB proteins differentially regulate LPS-induced inflammatory cytokine production in macrophages.
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“It has been reported that IκBNS that inhibits IL-6 production selectively in macrophages is induced by IL-10 and LPS [14].”
From Prolyl Isomerase Pin1 Protects Mice from Endotoxin Shock (2011) · cites this paper as [14]
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Cites
Janeway, C. A., & Medzhitov, R. (2002) · Annual Review of Immunology · doi:10.1146/annurev.immunol.20.083001.084359 · Cited by 8,394
Akira, S., & Takeda, K. (2004) · Nature reviews. Immunology · doi:10.1038/nri1391 · Cited by 8,312
Self-citationTakeda, K., Kaisho, T., & Akira, S. (2003) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141126 · Cited by 6,143
Self-citationAssociation of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
Hugot, J.-P., Chamaillard, M., Zouali, H., Lesage, S., Cézard, J.-P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C. A., Gassull, M., et al. (2001) · Nature · doi:10.1038/35079107 · Cited by 5,591
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
Ogura, Y., Bonen, D. K., Inohara, N., Nicolae, D. L., Chen, F. F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R. H., et al. (2001) · Nature · doi:10.1038/35079114 · Cited by 5,030
Toll-like receptors: critical proteins linking innate and acquired immunity
Akira, S., Takeda, K., & Kaisho, T. (2001) · Nature Immunology · doi:10.1038/90609 · Cited by 4,777
Self-citationInterleukin-10-deficient mice develop chronic enterocolitis
Kühn, R., Löhler, J., Rennick, D. M., Rajewsky, K., & Müller, W. (1993) · Cell · doi:10.1016/0092-8674(93)80068-p · Cited by 4,248
The immunological and genetic basis of inflammatory bowel disease
Bouma, G., & Strober, W. (2003) · Nature reviews. Immunology · doi:10.1038/nri1132 · Cited by 1,796
Akira, S. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.r300028200 · Cited by 1,499
Self-citationThe Immunology of Mucosal Models of Inflammation
Strober, W., Fuss, I. J., & Blumberg, R. S. (2002) · Annual Review of Immunology · doi:10.1146/annurev.immunol.20.100301.064816 · Cited by 1,317
Flagged first, then by citations
Research works printed but not linked: 40
- 1991, N. Engl. J. Med., 928
- 2002, Annu. Rev. Immunol., 495
- 2003, Nat. Rev. Immunol., 521
- Nat. Med., 567
- 2001, Nat. Immunol., 816
- 2003, J. Immunol., 3939
- 2002, Immunity, 219
- 2002, Annu. Rev. Immunol., 197
- 2001, Nat. Immunol., 675
- 2003, Annu. Rev. Immunol., 335
- 2004, Nat. Rev. Immunol., 499
- 1999, Immunity, 39
- 1993, Cell, 263
- 1996, J. Clin. Invest., 1010
- 2003, J. Clin. Invest., 1297
- 2001, Nature, 603
- 2001, Nature, 599
- 2003, Nat. Rev. Immunol., 371
- 2003, Gastroenterology, 148
- 2004, J. Immunol., 7377
- 2004, Nature, 218
- 2003, Blood, 4123
- 2002, J. Leukocyte Biol., 800
- 2000, Cytokine, 1312
- 2000, J. Leukocyte Biol., 97
- 2002, Mol. Cell., 637
- 1998, J. Virol., 8150
- 1993, Mol. Cell. Biol., 3557
- 2003, Eur. J. Immunol., 1073
- 1997, Eur. J. Gastroenterol. Hepatol., 893
- 1998, Gut, 1531
- 1989, Gut, 826
- 1988, Immunology, 543
- 1995, Gut, 367
- 1999, Clin. Exp. Immunol., 251
- 2002, J. Immunol., 2253
- 2001, J. Biol. Chem., 27657
- 2000, FEBS Lett., 53
- 2001, J. Biol. Chem., 12485
- 2004, Nat. Immunol., 800
Cited by
Sorted by citations
Items 101–167 of 167
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Annemann, M., Wang, Z., Plaza-Sirvent, C., Glauben, R., Schuster, M., Sander, F. E., Mamareli, P., Kühl, A., Siegmund, B., Lochner, M., et al. (2015) · Journal of Immunology · doi:10.4049/jimmunol.1401964 · Cited by 29
Matsumura, T., Oyama, M., Kozuka‐Hata, H., Ishikawa, K., Inoue, T., Muta, T., Semba, K., & Inoue, J. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.08.055 · Cited by 29
Toll-Like Receptor Signaling and Its Inducible Proteins
Satoh, T., & Akira, S. (2017) · ASM Press eBooks · doi:10.1128/9781555819194.ch24 · Cited by 29
Self-citationCytomegaloviruses and Macrophages—Friends and Foes From Early on?
Baasch, S., Ruzsics, Z., & Henneke, P. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00793 · Cited by 27
Zhou, Z., Ding, M., Huang, L., Gilkeson, G. S., Lang, R., & Jiang, W. (2016) · Clinical Immunology · doi:10.1016/j.clim.2016.09.005 · Cited by 27
Bain, C. C., Oliphant, C. J., Thomson, C. A., Kullberg, M. C., & Mowat, A. M. (2017) · Infection and Immunity · doi:10.1128/iai.00579-17 · Cited by 27
Bruserud, Ø. (2012) · Platelets · doi:10.3109/09537104.2012.678426 · Cited by 25
Sierra-Mondragón, E., Gómez‐Chávez, F., Murrieta-Coxca, J. M., Vázquez-Sánchez, E. A., Martínez-Torres, I., Cancino-Diaz, M. E., Rojas-Espinosa, O., Cancino‐Díaz, J. C., Reyes-Sánchez, J. L., Rodríguez‐Muñoz, R., et al. (2015) · Molecular Immunology · doi:10.1016/j.molimm.2015.09.020 · Cited by 24
The nuclear IκB family of proteins controls gene regulation and immune homeostasis
Maruyama, T. (2015) · International Immunopharmacology · doi:10.1016/j.intimp.2015.03.053 · Cited by 23
Ascochlorin induces caspase-independent necroptosis in LPS-stimulated RAW 264.7 macrophages
Park, J., Kim, H.-D., Lee, S.-H., Kwak, C.-H., Chang, Y., Lee, Y., Chung, T., Magae, J., & Kim, C. (2019) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2019.111898 · Cited by 23
Alternative nuclear functions for NF-κB family members.
Espinosa, L., Bigas, A., & Mulero, M. C. (2011) · Europe PMC (PubMed Central) · Cited by 22
Narimatsu, K., Higashiyama, M., Kurihara, C., Takajo, T., Maruta, K., Yasutake, Y., Sato, H., Okada, Y., Watanabe, C., Komoto, S., et al. (2015) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.12980 · Cited by 22
Dynamic chromatin association of IκBα is regulated by acetylation and cleavage of histone H4
Marruecos, L., Bertran, J., Villanueva, D. A., Mulero, M. C., Guillén, Y., Palma, L. G., Floor, M., Vert, A., Arce‐Gallego, S., Pecharromán, I., et al. (2021) · EMBO Reports · doi:10.15252/embr.202152649 · Cited by 21
Kohda, A., Yamazaki, S., & Sumimoto, H. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.719302 · Cited by 21
Yokota, M., Tamachi, T., Yokoyama, Y., Maezawa, Y., Takatori, H., Suto, A., Suzuki, K., Hirose, K., Takeda, K., & Nakajima, H. (2016) · Allergy · doi:10.1111/all.13079 · Cited by 20
Self-citationCibinetide dampens innate immune cell functions thus ameliorating the course of experimental colitis
Nairz, M., Haschka, D., Dichtl, S., Sonnweber, T., Schroll, A., Aßhoff, M., Mindur, J. E., Moser, P. L., Wolf, D. G. F., Świrski, F. K., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-13046-3 · Cited by 20
Immune Balance: The Development of the Idea and Its Applications
Świątczak, B. (2013) · Journal of the History of Biology · doi:10.1007/s10739-013-9370-z · Cited by 19
Kohda, A., Yamazaki, S., & Sumimoto, H. (2014) · Genes to Cells · doi:10.1111/gtc.12162 · Cited by 18
Takeda, K. (2005) · Japanese Journal of Clinical Immunology · doi:10.2177/jsci.28.309 · Cited by 18
Self-citationProlyl Isomerase Pin1 Protects Mice from Endotoxin Shock
Akiyama, H., Misawa, T., Ono, M., Uchida, C., & Uchida, T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0014656 · Cited by 17
Lost and Found: The Family of NF-κB Inhibitors Is Larger than Assumed in Salmonid Fish
van Muilekom, D. R., Collet, B., Rebl, H., Zlatina, K., Sarais, F., Goldammer, T., & Rebl, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210229 · Cited by 16
Hsa_circ_0007321 regulates Zika virus replication through miR-492/NFKBID/NF-κB signaling pathway
Kang, L., Xie, H., Ye, H., Jeyarajan, A. J., Warner, C. A., Huang, Y., Shi, Y., Li, Y., Yang, C., Xu, M., et al. (2023) · Journal of Virology · doi:10.1128/jvi.01232-23 · Cited by 17
Expression and localization of MrgprD in mouse intestinal tract
Zhou, C., Li, J., Liu, L., Tang, Z., Wan, F., & Lan, L. (2019) · Cell and Tissue Research · doi:10.1007/s00441-019-03017-7 · Cited by 16
The effective therapy of cyclosporine A with drug delivery system in experimental colitis
Fukata, N., Uchida, K., Kusuda, T., Koyabu, M., Miyoshi, H., Fukui, T., Matsushita, M., Nishio, A., Tabata, Y., & Okazaki, K. (2010) · Journal of drug targeting · doi:10.3109/1061186x.2010.511224 · Cited by 16
Dasgupta, S., & Kasper, D. L. (2010) · Advances in immunology · doi:10.1016/s0065-2776(10)06003-7 · Cited by 14
Chiba, T., Matsuzaka, Y., Warita, T., Sugoh, T., Miyashita, K., Tajima, A., Nakamura, M., Inoko, H., Sato, T., & Kimura, M. (2011) · Scandinavian Journal of Immunology · doi:10.1111/j.1365-3083.2011.02524.x · Cited by 14
Dwyer, J. R., Racine, J. J., Chapman, H. D., Quinlan, A., Presa, M. F., Stafford, G. A., Schmitz, I., & SERREZE, D. V. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100558 · Cited by 14
Umenai, T., Hirai, H., Shime, N., Nakaya, T., Asahara, T., Nomoto, K., Kita, M., Tanaka, Y., & Imanishi, J. (2010) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-010-0905-3 · Cited by 13
Intestinal Mononuclear Phagocytes in Health and Disease
Sanders, T. J., Yrlid, U., & Maloy, K. J. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0047-2016 · Cited by 13
Kurashina, R., Denda‐Nagai, K., Saba, K., Hisai, T., Hara, H., & Irimura, T. (2021) · Glycobiology · doi:10.1093/glycob/cwab015 · Cited by 12
Matsushima, H., Kumagai, Y., Vandenbon, A., Kataoka, H., Kadena, M., Fukamachi, H., Arimoto, T., Morisaki, H., Fujiwara, N., Okahashi, N., et al. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.02.048 · Cited by 12
Self-citationÁdori, M., Khoenkhoen, S., Zhang, J., Dopico, X. C., & Hedestam, G. B. K. (2023) · Cells · doi:10.3390/cells12091229 · Cited by 11
Pásztói, M., Pezoldt, J., & Huehn, J. (2015) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2015.07.012 · Cited by 10
Sun, X., & Feinberg, M. W. (2012) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.09.001 · Cited by 11
Altered Marginal Zone B Cell Selection in the Absence of IκBNS
Ádori, M., Pedersen, G. K., Ádori, C., Erikson, E., Khoenkhoen, S., Stark, J. M., Choi, J. H., Dosenovic, P., Karlsson, M. C. I., Beutler, B., et al. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700791 · Cited by 9
Kübelbeck, T., Wichmann, N. O., Raj, T., Raj, C., Ohnmacht, C., Hövelmeyer, N., Kramer, D., & Heissmeyer, V. (2025) · European Journal of Immunology · doi:10.1002/eji.202451273 · Cited by 8
Gross-Vered, M., Shmuel-Galia, L., Zarmi, B., Humphries, F., Thaiss, C. A., Salame, T., David, E., Chappell‐Maor, L., Fitzgerald, K. A., Shai, Y., et al. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900470 · Cited by 8
Kristek, M., Collins, L. E., DeCourcey, J., McEvoy, F., & Loscher, C. E. (2014) · Innate Immunity · doi:10.1177/1753425914538294 · Cited by 8
TACI expression and plasma cell differentiation are impaired in the absence of functional Iκ BNS
Khoenkhoen, S., Erikson, E., Ádori, M., Stark, J. M., Scholz, J. L., Cancro, M. P., Pedersen, G. K., & Hedestam, G. B. K. (2018) · Immunology and Cell Biology · doi:10.1111/imcb.12228 · Cited by 8
Frentzel, S., Jeron, A., Pausder, A., Kershaw, O., Volckmar, J., Schmitz, I., & Bruder, D. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1028789 · Cited by 6
Macrophage control of Crohn's disease
Tai, S. L., & Mortha, A. (2022) · International review of cytology · doi:10.1016/bs.ircmb.2022.01.003 · Cited by 5
IκBL, a novel member of the nuclear IκB family, inhibits inflammatory cytokine expression
Chiba, T., Miyashita, K., Sugoh, T., Warita, T., Inoko, H., Kimura, M., & Sato, T. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.10.024 · Cited by 5
Targeting Iκ BNS in allergic asthma: where it resides, matters
Sengupta, S., & Haczku, A. (2017) · Allergy · doi:10.1111/all.13126 · Cited by 4
Yu, H.-C., Huang, K., Lu, M., Tseng, H.-Y. H., Lai, N., & Huang, H. (2025) · Mediators of Inflammation · doi:10.1155/mi/8574340 · Cited by 3
Immunological Abnormalities in the Pathogenesis of Inflammatory Bowel Disease
Hisamatsu, T., Mikami, Y., Matsuoka, K., Kanai∥, T., & Hibi∥, T. (2012) · Intestinal Research · doi:10.5217/ir.2012.10.4.317 · Cited by 3
Kitamura, K., Isoda, K., Akita, K., Miyosawa, K., Kadoguchi, T., Shimada, K., & Daida, H. (2019) · IJC Heart & Vasculature · doi:10.1016/j.ijcha.2019.03.004 · Cited by 2
Changes in protein profiles of multiple myeloma cells in response to bortezomib
Turan, T., Şanlı‐Mohamed, G., & Baran, Y. (2012) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.3109/10428194.2012.735668 · Cited by 2
Physiological Role of TNF in Mucosal Immunology: Regulation of Macrophage/Dendritic Cell Function
Rivollier, A., Marsal, J., & Agace, W. W. (2015) · Frontiers of gastrointestinal research · doi:10.1159/000381381 · Cited by 1
Stewart, C. A., & Trinchieri, G. (2010) · Springer eBooks · doi:10.1007/978-1-4419-7219-4_4
Pneumovirus infection and effects on dendritic cells of mice
Arsic, N. (2008) · University Library - University of Saskatchewan (University of Saskatchewan)
Neurath, M. F. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-415847-4.00082-3
Intestinal macrophage, "a double-edged sword" for homeostasis and inflammation in the gut
Hisamatsu, T., Matsuoka, K., & Hibi∥, T. (2010) · Inflammation and Regeneration · doi:10.2492/inflammregen.30.412
Neonate Antigen Presenting Cells within Murine Intestinal Muscular Layer
Cruz-Morales, E., Meza‐Perez, S., Calderón‐Amador, J., Flores‐Langarica, A., & Flores‐Romo, L. (2011) · Immunological Investigations · doi:10.3109/08820139.2011.586394
Regulation of host immune responses by nuclear I.KAPPA.B proteins
Yamamoto, M., & Takeda, K. (2008) · Inflammation and Regeneration · doi:10.2492/inflammregen.28.516
Self-citationThe emerging roles of intestinal macrophages in sickness and in health
Kristek, M., & Loscher, C. E. (2014) · Hrčak Portal of scientific journals of Croatia (University Computing Centre)
Innate Immune Cells: Key Regulators of Homeostasis and Inflammation in Gut and Airway Mucosae
Töpfer, E., Gavigan-Imedio, J. D., Madej, M. P., Wilde, C. J., & Boraschi, D. (2014)
4. Recent Progress of Research and Clinics in Inflammatory Bowel Disease
Hibi∥, T., & Hisamatsu, T. (2013) · Nihon Naika Gakkai Zasshi · doi:10.2169/naika.102.2195
[Regulation of innate immune cell activity by IkappaBNS].
Takeda, K. (2006) · Folia Pharmacologica Japonica · doi:10.1254/fpj.128.68
Self-citationThe Intestinal Microbiome, the Immune System and Spondyloarthropathy
Costello, M., & Brown, M. A. (2017) · Springer eBooks · doi:10.1007/978-3-319-42252-7_8
Homeostatic control of IkappaB metabolism determines NF- kappaB responsiveness
O'Dea, E. L. (2010) · eScholarship (California Digital Library)
Tikka, C., Manthari, R. K., Niu, R., Sun, Z., & Wang, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.25.428065
Intestinal Mononuclear Phagocytes in Health and Disease
Sanders, T. J., Yrlid, U., & Maloy, K. J. (2017) · ASM Press eBooks · doi:10.1128/9781555819194.ch39
Endogenous Mediators of Neuroinflammation: The Endocannabinoid System at the Retina
Duraikkannu, D., & Chatterjee, N. (2022) · Springer eBooks · doi:10.1007/978-981-16-8313-8_25
Murray, P. J. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-374279-7.10011-6
Murray, P. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-128-24465-4.00032-6
核タンパク質IκBζはアンキリンリピートのN末端領域およびC末端領域を介してNF-κB p50およびLcn2プロモーターと転写活性化複合体を形成する
神田, 朗. (2017) · Institutional Repositories DataBase (IRDB) · doi:10.15017/1806886
Les lymphomes B diffus à grandes cellules de type activé : rôle de NF-κB et c-Myc.
Arnaud, N. (2017) · theses.fr (ABES) · doi:10.70675/f86c2a1cz9979z400dz8e23ze8914714a1a8
Metadata
- Authors
- Hirotani, T., Lee, P. Y., Kuwata, H., Yamamoto, M., Matsumoto, M., Kawase, I., Akira, S., & Takeda, K.
- Affiliations
- Research Institute for Microbial Diseases, The University of Osaka (JP)
- University of Florida Health (US)
- Kyushu University (JP)
- Japan Science and Technology Agency (JP)
- The University of Osaka (JP)
- Corresponding author
- Hirotani, Tomonori
- Yamamoto, Masahiro
- Akira, Shizuo
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 2005-03
- Volume
- 174
- Issue
- 6
- Pages
- 3650-3657
- ISSN
- 0022-1767 (ISSN-L)
- 1550-6606
- OpenAlex
- W1503222294
- Cited by
- 167
- References
- 42
- Citations by year
- 2025: 3 · 2024: 1 · 2023: 3 · 2022: 5 · 2021: 5 · 2020: 4 · 2019: 6 · 2018: 4 · 2017: 15 · 2016: 8 · 2015: 8 · 2014: 10 · 2013: 8 · 2012: 11
- FWCI
- 3.95
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Journal of Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
- Keywords
- Bcl-3, interleukin-6, TNF-α, lipopolysaccharide, macrophages, colonic lamina propria, IL-10, Toll-like receptor signaling, chronic colitis, IL-6 promoter
- MeSH terms
- Animals, Base Sequence, Cell Line, Colon, DNA, Humans, Intestinal Mucosa, Lipopolysaccharides, Macrophages, Mice, Inbred C57BL, Promoter Regions, Genetic, Protein Precursors, Proteins, Recombinant Proteins, Tumor Necrosis Factor-alpha, Interleukin-6, Gene Expression, NF-kappa B, Mice, Knockout, CD11b Antigen, Intracellular Signaling Peptides and Proteins, Mice, NF-kappa B p50 Subunit, In Vitro Techniques
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